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Items: 1 to 20 of 108

1.
2.

Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria.

Ware RE, Rosse WF, Howard TA.

Blood. 1994 May 1;83(9):2418-22.

3.

Structure and chromosomal localization of the GPI-anchor synthesis gene PIGF and its pseudogene psi PIGF.

Ohishi K, Inoue N, Endo Y, Fujita T, Takeda J, Kinoshita T.

Genomics. 1995 Oct 10;29(3):804-7.

PMID:
8575782
4.

Structures and chromosomal localizations of the glycosylphosphatidylinositol synthesis gene PIGC and its pseudogene PIGCP1.

Hong Y, Ohishi K, Inoue N, Endo Y, Fujita T, Takeda J, Kinoshita T.

Genomics. 1997 Sep 15;44(3):347-9.

PMID:
9325057
5.

Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease.

Nishimura J, Murakami Y, Kinoshita T.

Am J Hematol. 1999 Nov;62(3):175-82. Review.

6.

Paroxysmal nocturnal hemoglobinuria: insights from recent advances in molecular biology.

Bessler M, Schaefer A, Keller P.

Transfus Med Rev. 2001 Oct;15(4):255-67. Review.

PMID:
11668433
7.

Glycosyl phosphatidylinositol (GPI)-anchored molecules and the pathogenesis of paroxysmal nocturnal hemoglobinuria.

Boccuni P, Del Vecchio L, Di Noto R, Rotoli B.

Crit Rev Oncol Hematol. 2000 Jan;33(1):25-43. Review.

PMID:
10714960
8.

Glycosylphosphatidylinositol-anchor-deficient mice: implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria.

Kawagoe K, Kitamura D, Okabe M, Taniuchi I, Ikawa M, Watanabe T, Kinoshita T, Takeda J.

Blood. 1996 May 1;87(9):3600-6.

10.

Paroxysmal nocturnal hemoglobinuria: the price for a chance.

Bessler M.

Schweiz Med Wochenschr. 1996 Nov 9;126(45):1912-21. Review.

PMID:
8946596
12.

Impaired glycosylation of glycosylphosphatidylinositol-anchor synthesis in paroxysmal nocturnal hemoglobinuria leucocytes.

Hidaka M, Nagakura S, Horikawa K, Kawaguchi T, Iwamoto N, Kagimoto T, Takatsuki K, Nakakuma H.

Biochem Biophys Res Commun. 1993 Mar 15;191(2):571-9.

PMID:
8461014
13.
14.

Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early step.

Norris J, Hall S, Ware RE, Kamitani T, Chang HM, Yeh E, Rosse WF.

Blood. 1994 Feb 1;83(3):816-21.

15.
16.

Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria.

Yamada N, Miyata T, Maeda K, Kitani T, Takeda J, Kinoshita T.

Blood. 1995 Feb 15;85(4):885-92.

18.

Characterization of genomic PIG-A gene: a gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria.

Iida Y, Takeda J, Miyata T, Inoue N, Nishimura J, Kitani T, Maeda K, Kinoshita T.

Blood. 1994 Jun 1;83(11):3126-31.

19.

Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approaches.

Nishimura J, Smith CA, Phillips KL, Ware RE, Rosse WF.

Hematopathol Mol Hematol. 1998;11(3-4):119-46. Review.

PMID:
9844822
20.

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